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Standardized monitoring of cytomegalovirus-specific immunity can improve risk stratification of recurrent cytomegalovirus reactivation after hematopoietic stem cell transplantation
Wagner-Drouet, Eva Maria, Teschner, Daniel
, Wolschke, Christine, Janson, Dietlinde, Schäfer-Eckart, Kerstin, Gärtner, Johannes, Mielke, Stephan
, Schreder, Martin, Kobbe, Guido, Kondakci, Mustafa, Hilgendorf, Inken
, von Lilienfeld-Toal, Marie, Klein, Stefan, Heidenreich, Daniela, Kreil, Sebastian, Verbeek, Mareike, Graß, Sandra, Ditschkowski, Markus, Gromke, Tanja, Koch, Martina, Lindemann, Monika
, Hünig, Thomas, Schmidt, Traudel, Rascle, Anne
, Guldan, Harald, Barabas, Harald, Deml, Ludwig, Wagner, Ralf und Wolff, Daniel
(2021)
Standardized monitoring of cytomegalovirus-specific immunity can improve risk stratification of recurrent cytomegalovirus reactivation after hematopoietic stem cell transplantation.
Haematologica 106 (2), S. 363-374.
Veröffentlichungsdatum dieses Volltextes: 15 Mrz 2023 16:13
Artikel
DOI zum Zitieren dieses Dokuments: 10.5283/epub.45155
Zusammenfassung
Recurrence of cytomegalovirus reactivation remains a major cause of morbidity and mortality following allogeneic hematopoietic stem cell transplantation. Monitoring cytomegalovirus-specific cellular immunity using a standardized assay might improve the risk stratification of patients. A prospective multicenter study was conducted in 175 intermediate- and high-risk allogeneic hematopoietic stem ...
Recurrence of cytomegalovirus reactivation remains a major cause of morbidity and mortality following allogeneic hematopoietic stem cell transplantation. Monitoring cytomegalovirus-specific cellular immunity using a standardized assay might improve the risk stratification of patients. A prospective multicenter study was conducted in 175 intermediate- and high-risk allogeneic hematopoietic stem cell transplant recipients under preemptive antiviral therapy. Cytomegalovirus-specific cellular immunity was measured using a standardized interferon. enzyme-linked immunospot assay (T-Track (R) CMV). The primary aim was to evaluate the suitability of measuring cytomegalovirus-specific immunity after the end of treatment for a first cytomegalovirus reactivation to predict recurrent reactivation. Forty of 101 (39.6%) patients with a first cytomegalovirus reactivation experienced recurrent reactivations, mainly in the high-risk group (cytomegalovirus-seronegative donor/cytomegalovirus-seropositive recipient). The positive predictive value of T-Track (R) CMV (patients with a negative test after the first reactivation who experienced at least one recurrent reactivation) was 84.2% in high-risk patients. Kaplan-Meier analysis revealed a higher probability of recurrent cytomegalovirus reactivation in high-risk patients with a negative test after the first reactivation (hazard ratio 2.73; P=0.007). Interestingly, a post-hoc analysis considering T-Track (R) CMV measurements at day 100 after transplantation, a time point highly relevant for outpatient care, showed a positive predictive value of 90.0% in high-risk patients. Our results indicate that standardized cytomegalovirus-specific cellular immunity monitoring may allow improved risk stratification and management of recurrent cytomegalovirus reactivation after hematopoietic stem cell transplantation.
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| Dokumentenart | Artikel | ||||
| Titel eines Journals oder einer Zeitschrift | Haematologica | ||||
| Verlag: | Ferrata-Storti Foundation | ||||
|---|---|---|---|---|---|
| Ort der Veröffentlichung: | PAVIA | ||||
| Band: | 106 | ||||
| Nummer des Zeitschriftenheftes oder des Kapitels: | 2 | ||||
| Seitenbereich: | S. 363-374 | ||||
| Datum | Februar 2021 | ||||
| Institutionen | Medizin > Lehrstuhl für Innere Medizin III (Hämatologie und Internistische Onkologie) Medizin > Lehrstuhl für Medizinische Mikrobiologie und Hygiene | ||||
| Identifikationsnummer |
| ||||
| Stichwörter / Keywords | CD8(+) T-CELLS; IDENTIFY PATIENTS; QUANTIFERON-CMV; RECONSTITUTION; RECIPIENTS; INFECTION; DISEASE; CD4(+); RESPONSES; ASSAY; | ||||
| Dewey-Dezimal-Klassifikation | 600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin | ||||
| Status | Veröffentlicht | ||||
| Begutachtet | Ja, diese Version wurde begutachtet | ||||
| An der Universität Regensburg entstanden | Ja | ||||
| URN der UB Regensburg | urn:nbn:de:bvb:355-epub-451554 | ||||
| Dokumenten-ID | 45155 |
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